Canonical Allele Identifier: CA433356055
Gene: LYZL4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.42448375G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.42406883G>C , CM000665.2:g.42406883G>C GRCh38
NC_000003.11:g.42448375G>C , CM000665.1:g.42448375G>C GRCh37
NC_000003.10:g.42423379G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000287748.8:c.255C>G MANE Select ENSP00000287748.3:p.Gly85=
ENST00000287748.7:c.255C>G ENSP00000287748.3:p.Gly85=
ENST00000441172.1:c.255C>G ENSP00000387897.1:p.Gly85=
ENST00000470991.1:n.285C>G
NM_001304386.1:c.255C>G NP_001291315.1:p.Gly85=
NM_144634.3:c.255C>G NP_653235.1:p.Gly85=
XM_011533355.1:c.255C>G XP_011531657.1:p.Gly85=
XM_011533355.3:c.255C>G XP_011531657.1:p.Gly85=
XM_017005706.1:c.255C>G XP_016861195.1:p.Gly85=
XM_024453345.1:c.255C>G XP_024309113.1:p.Gly85=
NM_144634.4:c.255C>G MANE Select NP_653235.1:p.Gly85=
NM_001304386.2:c.255C>G NP_001291315.1:p.Gly85=